Partial deletion of 18p and partial duplication of 18q caused by a paternal pericentric inversion

Clinical Genetics

Volumn 50, Issue 6, 1996, Pages 520-524

  Israëls, Trijn ^a,c   Hoovers, Jan ^a   Turpijn, Hanne M ^b   Wijburg, Frits A ^a   Hennekam, Raoul C M ^a  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

^b BovenIJ Ziekenhuis   (Netherlands)

^c EMMA CHILDREN S HOSPITAL   (Netherlands)

Author keywords

Chromosome 18; Inversion, partial monosomy 18p; Partial trisomy 18q; Pericentric; Recombinant chromosome; Stridor

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 18P; CHROMOSOME 18Q; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CLINICAL FEATURE; FATHER; HUMAN; HUMAN CELL; MALE; PERICENTRIC CHROMOSOME INVERSION; PRIORITY JOURNAL; STRIDOR; SYNDROME DELINEATION;

EID: 0030455386     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1996.tb02726.x     Document Type: Article

References (17)

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